Status: current, Sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2018. Module: SNOMED CT core
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 3644020014 | Megakaryoblastic acute myeloid leukaemia with t(1;22)(p13;q13) | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 3644021013 | Megakaryoblastic acute myeloid leukemia with t(1;22)(p13;q13) (disorder) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 3644022018 | Megakaryoblastic acute myeloid leukemia with t(1;22)(p13;q13) | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 766571000241115 | leucémie myéloïde aigüe mégacaryoblastique associée à t(1;22)(p13;q13) (trouble) | fr | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT Common French translation module (core metadata concept) |
| 891461000172110 | leucémie myéloïde aigüe mégacaryoblastique associée à t(1;22)(p13;q13) | fr | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT Common French translation module (core metadata concept) |
| 3644023011 | A rare subtype of acute myeloid leukemia with recurrent cytogenetic abnormalities characterized by clonal proliferation of myeloid blasts with predominantly megakaryoblastic differentiation in the bone marrow and blood, often with extensive infiltration of the abdominal organs. It occurs typically in infants and usually presents with hepatosplenomegaly, anemia, thrombocytopenia and nonspecific symptoms related to ineffective hematopoesis (fatigue, bleeding and bruising, recurrent infections). Myelofibrosis and fibrosis of other infiltrated organs is also characteristic of this disease. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| 3644024017 | A rare subtype of acute myeloid leukaemia with recurrent cytogenetic abnormalities characterised by clonal proliferation of myeloid blasts with predominantly megakaryoblastic differentiation in the bone marrow and blood, often with extensive infiltration of the abdominal organs. It occurs typically in infants and usually presents with hepatosplenomegaly, anaemia, thrombocytopenia and nonspecific symptoms related to ineffective haematopoesis (fatigue, bleeding and bruising, recurrent infections). Myelofibrosis and fibrosis of other infiltrated organs is also characteristic of this disease. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Megakaryoblastic acute myeloid leukaemia with t(1;22)(p13;q13) | est un(e) (attribut) | Acute myeloid leukemia due to recurrent genetic abnormality (disorder) | true | Inferred relationship | Some | ||
| Megakaryoblastic acute myeloid leukaemia with t(1;22)(p13;q13) | morphologie associée (attribut) | Acute myeloid leukaemia (megakaryoblastic) with t(1;22)(p13;q13); RBM15-MKL1 | true | Inferred relationship | Some | 1 | |
| Megakaryoblastic acute myeloid leukaemia with t(1;22)(p13;q13) | localisation d'une constatation (attribut) | Bone marrow structure | true | Inferred relationship | Some | 1 |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
This concept is not in any reference sets
FHIR